Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Recalls
- Mar 24, 2016 · Class III · Lupin Limited
Labeling: Incorrect or Missing Lot and/or Expiration Date
Lots: Lot # G510086; Exp. 11/17
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078169
- On the market since
- Sep 10, 2012
- Package NDCs
68180-137-0168180-137-06- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?